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Identification of the anti-tumor activity and mechanisms of nuciferine through a network pharmacology approach.
- Source :
-
Acta pharmacologica Sinica [Acta Pharmacol Sin] 2016 Jul; Vol. 37 (7), pp. 963-72. Date of Electronic Publication: 2016 May 16. - Publication Year :
- 2016
-
Abstract
- Aim: Nuciferine is an aporphine alkaloid extracted from lotus leaves, which is a raw material in Chinese medicinal herb for weight loss. In this study we used a network pharmacology approach to identify the anti-tumor activity of nuciferine and the underlying mechanisms.<br />Methods: The pharmacological activities and mechanisms of nuciferine were identified through target profile prediction, clustering analysis and functional enrichment analysis using our traditional Chinese medicine (TCM) network pharmacology platform. The anti-tumor activity of nuciferine was validated by in vitro and in vivo experiments. The anti-tumor mechanisms of nuciferine were predicted through network target analysis and verified by in vitro experiments.<br />Results: The nuciferine target profile was enriched with signaling pathways and biological functions, including "regulation of lipase activity", "response to nicotine" and "regulation of cell proliferation". Target profile clustering results suggested that nuciferine to exert anti-tumor effect. In experimental validation, nuciferine (0.8 mg/mL) markedly inhibited the viability of human neuroblastoma SY5Y cells and mouse colorectal cancer CT26 cells in vitro, and nuciferine (0.05 mg/mL) significantly suppressed the invasion of 6 cancer cell lines in vitro. Intraperitoneal injection of nuciferine (9.5 mg/mL, ip, 3 times a week for 3 weeks) significantly decreased the weight of SY5Y and CT26 tumor xenografts in nude mice. Network target analysis and experimental validation in SY5Y and CT26 cells showed that the anti-tumor effect of nuciferine was mediated through inhibiting the PI3K-AKT signaling pathway and IL-1 levels in SY5Y and CT26 cells.<br />Conclusion: By using a TCM network pharmacology method, nuciferine is identified as an anti-tumor agent against human neuroblastoma and mouse colorectal cancer in vitro and in vivo, through inhibiting the PI3K-AKT signaling pathways and IL-1 levels.
- Subjects :
- Animals
Cell Line, Tumor
Cell Survival drug effects
Class I Phosphatidylinositol 3-Kinases
Cluster Analysis
Drugs, Chinese Herbal pharmacology
Humans
Mice
Mice, Nude
Neoplasm Invasiveness
Phosphatidylinositol 3-Kinases metabolism
Xenograft Model Antitumor Assays
Antineoplastic Agents pharmacology
Aporphines pharmacology
Signal Transduction drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1745-7254
- Volume :
- 37
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Acta pharmacologica Sinica
- Publication Type :
- Academic Journal
- Accession number :
- 27180984
- Full Text :
- https://doi.org/10.1038/aps.2016.53